Iotamotion, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories1
Latest Approval2026-01-09
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K252339 | iotaSOFT® Insertion System | QQH | 2026-01-09 | View |
| 510(k) | DEN190055 | iotaSOFT Insertion System - Drive Unit, Controller and Accessories | QQH | 2021-10-01 | View |
No matching devices.